ABBA: Analysis of Blood-based Biomarkers of Asthma

Sponsor
University of California, San Francisco (Other)
Overall Status
Completed
CT.gov ID
NCT00917787
Collaborator
Genentech, Inc. (Industry)
127
1
22
5.8

Study Details

Study Description

Brief Summary

The purpose of this study is to analyze markers of inflammation in blood and in induced sputum for the purpose of identifying molecular markers of specific asthma phenotypes. The investigators' specific interest is demonstrating that periostin levels are higher than normal in blood. The investigators already have solid preliminary data to support this hypothesis, and our goal here is to replicate preliminary findings and extend them by examining further the characteristics of the asthma subgroup with elevated periostin levels.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    This is a cross-sectional study in patients with asthma and healthy controls in which we will analyze markers of inflammation in blood and in induced sputum for the purpose of identifying molecular markers of specific asthma phenotypes. Our specific interest in demonstrating that periostin levels are higher than normal in blood. We already have solid preliminary data to support this hypothesis, and our goal here is to replicate preliminary findings and extend them by examining further the characteristics of the asthma subgroup with elevated periostin levels. In this regard, we propose detailed phenotyping of the asthmatic subjects and the healthy controls, including measures in induced sputum, exhaled air and detailed physiologic measures including measures of airflow, lung volumes, and methacholine responsiveness. In earlier work we have found that periostin is a marker of Th-2 driven asthma, and we will use the data collected here to further explore this possibility. The biospecimens collected here will also allow us to expand existing plasma, DNA, RNA, and sputum samples in the UCSF Airway tissue bank, so that we can continue to build this resource for future research questions.

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    127 participants
    Observational Model:
    Cohort
    Time Perspective:
    Cross-Sectional
    Official Title:
    Analysis of Blood-based Biomarkers of Asthma
    Study Start Date :
    Jun 1, 2009
    Actual Primary Completion Date :
    Apr 1, 2011
    Actual Study Completion Date :
    Apr 1, 2011

    Arms and Interventions

    Arm Intervention/Treatment
    Healthy, Non-asthmatic

    Asthma

    Outcome Measures

    Primary Outcome Measures

    1. periostin levels in blood [1 week]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 70 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes

    Asthmatic Subjects Inclusion criteria

    1. Male and female subjects between the ages of 18 and 70 years with a history of asthma who may or may not be taking inhaled corticosteroids for asthma control.

    2. Physician diagnosis of asthma

    3. PC20FEV1 methacholine ≤ 8.0 mg/mL, except for those taking daily inhaled corticosteroids, for which the PC20 methacholine should be < 16 mg/mL.

    4. Ability to provide informed consent.

    Healthy Subjects Inclusion criteria

    1. Healthy male and female subjects with no history of asthma between the ages of 18 and 70 years. Subjects should not be taking inhaled or oral corticosteroids.

    2. No lifetime history of asthma or allergic rhinitis.

    3. Ability to provide informed consent.

    Exclusion Criteria for both subject groups

    1. Lung disease other than asthma.

    2. History of an upper or lower respiratory tract infection in the 4 weeks preceding the study.

    3. Females who are pregnant or breast-feeding

    4. Subjects must be non-smokers (patients who have never smoked or patients who have smoked ≤5 cigarettes per month and have a total pack-year smoking history < 10 packs).

    5. Use of marijuana >1 time per month in the last year and use of marijuana in the 6 weeks prior to enrollment

    6. Use of recreational drugs other than marijuana in the 12 months preceding the study.

    7. Use of Beta blocker medications

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 UCSF Airway Clinical Research Center San Francisco California United States 94143-0130

    Sponsors and Collaborators

    • University of California, San Francisco
    • Genentech, Inc.

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    University of California, San Francisco
    ClinicalTrials.gov Identifier:
    NCT00917787
    Other Study ID Numbers:
    • H6788-34128-01
    First Posted:
    Jun 10, 2009
    Last Update Posted:
    Aug 20, 2020
    Last Verified:
    Aug 1, 2020
    Keywords provided by University of California, San Francisco
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Aug 20, 2020